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Evaluation of the Frequency of Limitation of Activity in Patients With Persistent Asthma (ASMAVIE)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01078688
First Posted: March 2, 2010
Last Update Posted: January 29, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
AstraZeneca
  Purpose
Evaluation of the frequency of limitation of activity, depending on gender and age-group, in patients with persistent asthma consulting a general practitioner

Condition
Persistent Asthma

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Evaluation of the Frequency of Limitation of Activity, Depending on Gender and Age-group, in Patients With Persistent Asthma Consulting a General Practitioner

Resource links provided by NLM:


Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • To describe the frequency of limitations of activities in patients with persistent asthma depending on gender and age-group. [ Time Frame: Last 3 months / once ]
  • To describe, depending on gender and age-group, the nature of the activities limited, the degree of limitation and the impact on the patient's daily life. [ Time Frame: Once during only visit ]

Secondary Outcome Measures:
  • To describe the nature of the activities limited, the degree of limitation and the impact on the patient's daily life according to the level of asthma control [ Time Frame: Once during only visit ]
  • To describe, depending on gender and age-group, the activities that need to be specifically investigated in routine clinical practice due to their greater impact on the patient's quality of life, and which could indicate poorly controlled asthma [ Time Frame: Once during only visit ]
  • To describe the main characteristics and initial management for all patients of the survey [ Time Frame: Once during only visit ]

Enrollment: 1942
Study Start Date: March 2010
Study Completion Date: October 2010
Primary Completion Date: October 2010 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
First 3 consecutive patients with persistent asthma seen by general practitioner receiving long-term maintenance treatment with inhaled steroids
Criteria

Inclusion Criteria:

  • persistent asthma receiving long-term maintenance treatment with inhaled steroids (alone or in combination with other drugs)

Exclusion Criteria:

  • Patients with a diagnosis of COPD
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01078688


  Show 728 Study Locations
Sponsors and Collaborators
AstraZeneca
Investigators
Study Director: Pascal Piedbois AstraZeneca
  More Information

Responsible Party: AstraZeneca
ClinicalTrials.gov Identifier: NCT01078688     History of Changes
Other Study ID Numbers: NIS-RFR-DUM-2009/2
First Submitted: February 25, 2010
First Posted: March 2, 2010
Last Update Posted: January 29, 2013
Last Verified: January 2013

Keywords provided by AstraZeneca:
Limitations of activities
persistent asthma
general practitioner
frequency of limitations of activities
depending on gender and age-group

Additional relevant MeSH terms:
Asthma
Bronchial Diseases
Respiratory Tract Diseases
Lung Diseases, Obstructive
Lung Diseases
Respiratory Hypersensitivity
Hypersensitivity, Immediate
Hypersensitivity
Immune System Diseases